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Adenosine modulates oesophageal sensorimotor function in humans.

J M Remes-Troche1, P Chahal, R Mudipalli

  • 1Department of Internal Medicine, Division of Gastroenterology-Hepatology, Section of Neurogastroenterology, University of Iowa Carver College of Medicine & Clinical Research Center, Iowa City, Iowa 52242, USA.

Gut
|February 21, 2008
PubMed
Summary
This summary is machine-generated.

Adenosine infusion in healthy volunteers significantly lowered pain perception thresholds and decreased esophageal distensibility. These findings suggest adenosine plays a role in functional chest pain by altering esophageal sensorimotor function.

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Area of Science:

  • Gastroenterology
  • Neuroscience
  • Physiology

Background:

  • Adenosine is known to mediate pain but its role in gut visceral nociception is not well understood.
  • The specific effects of adenosine on esophageal sensorimotor function required investigation.

Purpose of the Study:

  • To investigate the hypothesis that adenosine alters esophageal sensorimotor function.
  • To assess adenosine's impact on visceral nociception in the esophagus.

Main Methods:

  • A double-blind, randomized, placebo-controlled study involving 14 healthy volunteers.
  • Intravenous administration of adenosine or placebo, followed by stepwise esophageal balloon distensions using impedance planimetry.
  • Assessment of sensory responses and biomechanical properties of the esophagus.

Main Results:

  • Adenosine significantly reduced thresholds for esophageal perception, discomfort, and pain compared to placebo.
  • Lowered median threshold pressures were observed for first perception, discomfort, and pain after adenosine infusion.
  • Adenosine increased esophageal cross-sectional area and stiffened the esophageal wall.

Conclusions:

  • Adenosine induces visceral hyperalgesia and reduces esophageal distensibility in humans.
  • The observed sensorimotor changes mimic those in patients with functional esophageal chest pain.
  • Adenosine modulates esophageal sensorimotor function and may contribute to the pathogenesis of functional chest pain.